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Research 601–630 of 1000+
- Itchy Black Hair Bristles on Back
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Current Status of the Applications of Conditioned Media Derived from Mesenchymal Stem Cells for Regenerative Medicine
- Analogs of human genetic skin disease in domesticated animals
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- New-Onset Gastrointestinal Polyposis
- Creatine phosphokinase levels and isotretinoin therapy
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Primary cicatricial alopecia and inflammatory bowel disease – is there a link?
- Advances in Dermatology
- Hair Replacement. Dow B. Stough and Robert S. Haber. St. Louis: Mosby, 1995. 448 pages. Price $189.00.
- Progeroide Syndrome
- Pharmacologic Therapy of Polycystic Ovary Syndrome
- Trichoscopy in Hair Shaft Disorders
- Treatment of multiple scalp basal cell carcinomas by photodynamic therapy
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Manual of chemical peels: Superficial and medium depth
- Low level of high-density lipoprotein cholesterol is solely associated with greater severity of male androgenetic alopecia: A cross-sectional study of Thai population
- Cutaneous manifestations of HIV infection other than Kaposi's sarcoma: Clinical and histologic aspects
- Endocrine-skin interactions
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- WISP-1 induced by mechanical stress contributes to fibrosis and hypertrophy of the ligamentum flavum through Hedgehog-Gli1 signaling
- Hair-Thread Tourniquet Syndrome: A Case Report and Literature Review
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair Shaft Dysplasias
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta